About Deletion 5q35 syndrome
Deletion 5q35 syndrome is a rare disease catalogued by Orphanet (ORPHA:1627). It is associated with the NKX2-5, NSD1 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Deletion 5q35 syndrome trials.
Search ClinicalTrials.gov for "Deletion 5q35 syndrome" or filter by Orphanet code ORPHA:1627 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Deletion 5q35 syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Deletion 5q35 syndrome. Updated daily.